58819-72-0 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,6-Dimethoxypyridine-3-carboxaldehyde is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties.
Used in Organic Synthesis:
2 6-DIMETHOXYPYRIDINE-3-CARBOXALDEHYDE& serves as a building block in organic synthesis, enabling the preparation of various compounds with diverse applications. Its reactivity and functional groups make it a valuable component in the creation of complex organic molecules.
Used in Medicinal Chemistry Research:
2,6-Dimethoxypyridine-3-carboxaldehyde has been studied for its potential biological activities, making it a compound of interest in medicinal chemistry research. Its exploration may lead to the discovery of new drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 58819-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,1 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58819-72:
(7*5)+(6*8)+(5*8)+(4*1)+(3*9)+(2*7)+(1*2)=170
170 % 10 = 0
So 58819-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3/c1-11-7-4-3-6(5-10)8(9-7)12-2/h3-5H,1-2H3
58819-72-0Relevant academic research and scientific papers
Transformations of trichloromethyl groups during reactions of 3-trichloromethylpyridines with methoxide
Dainter, Ronald S.,Jackson, Tracey,Omar, Abdirahman H. H.,Suschitzky, Hans,Wakefield, Basil J.,Hughes, Nigel,Nelson, Anthony J.,Varvounis, George
, p. 283 - 287 (2007/10/02)
When methoxide ion attacks an unsubstituted 2- or 6-position of a 3-trichloromethylpyridine, a hydrogen shift leads to a methoxy-substituted 3-dichloromethylpyridine. Further reaction of the dichloromethyl group with methoxide gives the corresponding acetal. This type of reaction has been applied to several chlorinated 3-trichloromethylpyridines and to 3- trichloromethylpyridine itself; a convenient synthesis of the latter is described.
ABNORMAL NUCLEOPHILIC SUBSTITUTION OF 3-TRICHLOROMETHYLPYRIDINES BY METHOXIDE
Dainter, Ronald S.,Suschitzky, Hans,Wakefield, Basil J.,Hughes, Nigel,Nelson, Anthony J.
, p. 5693 - 5696 (2007/10/02)
3-Trichloromethylpyridine and its α-chlorinated derivatives behave as ambident electrophilic substrates towards methoxide which attacks an α-position and the trichloromethyl group.
